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US9480992B2ActiveUtilityPatentIndex 42

Method for the separation of polarizable bioparticles

Assignee: SCHMID ANDREASPriority: May 10, 2011Filed: May 9, 2012Granted: Nov 1, 2016
Est. expiryMay 10, 2031(~4.9 yrs left)· nominal 20-yr term from priority
Inventors:SCHMID ANDREASBLANK LARS MHOWITZ STEFFENFRITZSCH FREDERIK SVEN OLE
B03C 5/005B81B 7/02B01L 2400/0424B03C 2201/26B03C 5/026B01L 3/50273
42
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Claims

Abstract

The invention relates to a method for the separation of a polarizable bioparticle comprising the steps: a) dielectrophoretic preseparation of a polarizable bioparticle from a suspension of bioparticles; b) fluidic separation of the selected bioparticle by fixing the bioparticle in a dielectrophoretic field cage and circulating fluid around the bioparticle; c) transferring the separated bioparticle from the dielectrophoretic field cage to a culture chamber; d) dielectrophoretic fixing of the separated bioparticle in the culture chamber and study, observation, manipulation and/or culturing of the separated bioparticle. The invention further relates to a microfluidic system and use thereof.

Claims

exact text as granted — not AI-modified
The invention claimed is: 
     
       1. A method for the separation of a single polarizable bioparticle with a microfluidic system, comprising the following steps:
 a) dielectrophoretic preseparation of the polarizable bioparticle from a suspension of bioparticles; 
 b) fluidic separation of the polarizable bioparticle selected in step a) by trapping the polarizable bioparticle in a dielectrophoretic field cage and circulating fluid around the polarizable bioparticle; 
 c) transfer of the polarizable bioparticle separated in step b) out of the dielectrophoretic field cage into a cultivation chamber; and 
 d) dielectrophoretic trapping of the polarizable bioparticle separated in step b) in the cultivation chamber and study, observation, manipulation and/or cultivation of the polarizable bioparticle, wherein the polarizable bioparticle has a diameter in the range of ≧0.5 μm to ≦5 μm. 
 
     
     
       2. The method of  claim 1 , wherein analytes of the polarizable bioparticle separated in step b) are removed from the cultivation chamber for analysis. 
     
     
       3. The method of  claim 2 , wherein the analyte or analytes of the polarizable bioparticle separated in step b) are analyzed by optical and/or non-optical methods. 
     
     
       4. The method of  claim 1 , wherein the dielectrophoretic trapping of the polarizable bioparticle separated in step b) in the cultivation chamber occurs in a further dielectrophoretic field cage and/or by means of an electrode arrangement. 
     
     
       5. The method of  claim 1 , wherein, after study, observation and/or manipulation, the polarizable bioparticle separated in step b) is led away alive for propagation in a population.

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